A high-performance aqueous rechargeable zinc battery based on organic cathode integrating quinone and pyrazine

电化学 阴极 法拉第效率 吡嗪 材料科学 电池(电) 水溶液 化学工程 电极 纳米技术 物理化学 有机化学 化学 功率(物理) 冶金 工程类 物理 量子力学
作者
Yingjie Gao,Gaofeng Li,Feng Wang,Jun Chu,Yu Pu,Baoshan Wang,Hui Zhan,Zhiping Song
出处
期刊:Energy Storage Materials [Elsevier]
卷期号:40: 31-40 被引量:227
标识
DOI:10.1016/j.ensm.2021.05.002
摘要

In spite of the recent rapid progress of organic cathode materials for aqueous rechargeable zinc batteries (ARZBs), there are still many challenges such as unaffordable synthesis, unsatisfactory electrochemical performance, and unclear mechanisms in this field. Herein, we report 5,7,12,14-tetraaza-6,13-pentacenequinone (TAPQ) as an easily-synthesized organic cathode material with a novel quinone/pyrazine hybrid structure. Benefitting from the multiple electroactive C=O and C=N bonds, TAPQ possessed a theoretical capacity of 515 mAh g–1 (based on a six-electron reaction) and a practically reversible capacity of 443 mAh g–1 within 0.1–1.6 V vs. Zn2+/Zn, both of which set new records for organic cathodes in ARZBs. The H+/Zn2+ co-insertion mechanism involving H+ as the predominant participant was confirmed by detailed investigations including various ex-situ characterizations, electrochemical tests, and DFT calculations. Based on the clear mechanism understanding, a modified voltage range of 0.5–1.6 V was adopted to simultaneously achieve high energy density (270 mAh g–1 × 0.84 V = 227 Wh kg–1) and excellent cycling stability (capacity retention of 92% after 250 cycles under 50 mA g–1, with an average Coulombic efficiency of 99.96%). Furthermore, the evolution mechanism of TAPQ electrode structure during cycling was also carefully studied to reveal the origin of capacity decline. The novel molecular structure, easy synthesis, superior electrochemical performance, and deeper mechanism understanding provide researchers important insights into the further development of organic cathode materials for ARZBs toward practical applications.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
酷波er应助典雅的飞丹采纳,获得10
刚刚
壮观溪流发布了新的文献求助10
刚刚
大模型应助张nmky采纳,获得10
1秒前
1秒前
2秒前
2秒前
5秒前
5秒前
6秒前
道消完成签到,获得积分10
6秒前
聪明邪欢发布了新的文献求助10
7秒前
面壁思过发布了新的文献求助10
7秒前
9秒前
云阿柔完成签到,获得积分10
9秒前
11秒前
朴实雪兰发布了新的文献求助10
12秒前
13秒前
科研通AI6应助欣欣采纳,获得10
13秒前
13秒前
shijie应助武慧丹采纳,获得10
15秒前
素衣发布了新的文献求助10
16秒前
弄香完成签到,获得积分10
16秒前
无限安荷发布了新的文献求助10
16秒前
浮游应助王手采纳,获得10
19秒前
浮游应助江浔卿采纳,获得10
19秒前
cheung发布了新的文献求助10
20秒前
林岚完成签到,获得积分10
21秒前
22秒前
23秒前
司空元正完成签到 ,获得积分10
24秒前
科目三应助科研通管家采纳,获得10
25秒前
Akim应助科研通管家采纳,获得10
25秒前
英俊的铭应助科研通管家采纳,获得10
25秒前
NexusExplorer应助科研通管家采纳,获得10
25秒前
AN应助科研通管家采纳,获得30
25秒前
科目三应助科研通管家采纳,获得10
25秒前
浮游应助科研通管家采纳,获得10
25秒前
浮游应助科研通管家采纳,获得10
25秒前
酷波er应助科研通管家采纳,获得10
25秒前
25秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
List of 1,091 Public Pension Profiles by Region 1601
Lloyd's Register of Shipping's Approach to the Control of Incidents of Brittle Fracture in Ship Structures 800
Biology of the Reptilia. Volume 21. Morphology I. The Skull and Appendicular Locomotor Apparatus of Lepidosauria 620
A Guide to Genetic Counseling, 3rd Edition 500
Laryngeal Mask Anesthesia: Principles and Practice. 2nd ed 500
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5557467
求助须知:如何正确求助?哪些是违规求助? 4642491
关于积分的说明 14668341
捐赠科研通 4583911
什么是DOI,文献DOI怎么找? 2514433
邀请新用户注册赠送积分活动 1488818
关于科研通互助平台的介绍 1459439